TrellOss-L MPF
K-Number: K192687 · 2020-01-09
ApplicantNexxt Spine, LLC
Decision Date2020-01-09
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
TrellOss-L MPF is a medical device manufactured by Nexxt Spine, LLC. It received FDA 510(k) clearance on 2020-01-09 under approval number K192687. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TrellOss-L MPF?
TrellOss-L MPF is a medical device that received FDA 510(k) clearance on 2020-01-09. It is manufactured by Nexxt Spine, LLC. The 510(k) number is K192687.
When was TrellOss-L MPF approved by the FDA?
TrellOss-L MPF received FDA 510(k) clearance on 2020-01-09, under approval number K192687.
What company makes TrellOss-L MPF?
TrellOss-L MPF is manufactured by Nexxt Spine, LLC.
What is the FDA product code for TrellOss-L MPF?
The FDA product code for TrellOss-L MPF is MAX.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.